Methods for producing solvents derived from 1-chloro-3, 3, 3-trifluoro-propene (1233zd)

ABSTRACT

The production of solvents for applications such as heat transfer, cleaning, and degreasing, for example. In particular, the production of solvents derived from 1-chloro-3,3,3-trifluoro-propene, such as chloro and/or fluoro substituted alkanes and chloro and/or fluoro substituted trifluoropropenyl ethers.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a divisional application of U.S. patent application Ser. No. 15/606,400, filed on May 26, 2017, entitled METHODS FOR PRODUCING SOLVENTS DERIVED FROM 1-CHLORO-3,3,3-TRIFLUORO-PROPENE (1233ZD), which claims the benefit under Title 35, U.S.C. § 119(e) of U.S. Provisional Patent Application Ser. No. 62/345,117, entitled METHODS FOR PRODUCING SOLVENTS DERIVED FROM 1-CHLORO-3,3,3-TRIFLUORO-PROPENE (1233zd), filed on Jun. 3, 2016, the entire disclosure of which is expressly incorporated by reference herein.

BACKGROUND

The present disclosure relates to the production of solvents for use in applications such as heat transfer, cleaning and degreasing, for example and, in particular, the present disclosure relates to the production of solvents that are derived from 1-chloro-3,3,3-trifluoro-propene.

1-chloro-3,3,3-trifluoro-propene (CF₃CH═CHCl, also known as 1233zd) may be used as heat transfer fluid, as well as a cleaning solvent or a carrier solvent. Advantageously, 1233zd is non-flammable, has a low global warming potential (GWP), and low toxicity. 1233zd is also an effective solvent for a number of organic substances, such as different kinds of oils and greases, making 1233zd useful as a cleaning and degreasing solvent.

However, because 1233zd has a low boiling point (19° C. for the trans isomer), when 1233zd is used as a solvent, challenges are presented in connection with handling and operation. For example, 1233zd is typically transported and dispensed from a high pressure cylinder package, which may be costly and may require complex process integration steps with existing machinery and tooling, as well as training of personnel. The low boiling point of 1233zd may also result in higher vapor loss, potentially leading to a higher rate of consumption. In addition to potential challenges relating to the low boiling point of 1233zd, there is some concern in certain use applications regarding the chlorine atom in the molecule, for example, in the electronics manufacturing industry where halogen-free reagents and solvents may be desired.

Solvents based on 1233zd which exhibit one or more of the properties of non-chlorine containing, low GWP, low toxicity, and non-flammability are desired.

SUMMARY

The present disclosure relates to the production of solvents for applications such as heat transfer, cleaning, and degreasing, for example. In particular, the present disclosure relates the production of solvents derived from 1-chloro-3,3,3-trifluoro-propene, such as chloro and/or fluoro substituted alkanes and chloro and/or fluoro substituted trifluoropropenyl ethers.

In one form thereof, the present disclosure provides a method for producing a product according to one of formulas: CF₃—CH₂—CHCl—O—C_(n)H_(x)F_(y)Cl_(z) and CF₃—CH═CH—O—C_(n)H_(x)F_(y)Cl_(z)

wherein:

n is 1 to 5;

x, y, and z are each 0 to 11 and y+z≥1; and

x+y+z=2(n−m)+1, wherein m is an integer of 0 to 2, the method comprising the step of reacting a reaction mixture including an alcohol, a catalyst, and 1-chloro-3,3,3-trifluoro-propene (1233zd).

The alcohol may be an alcohol according to the following formula: C_(n)H_(x)F_(y)Cl_(z)OH

wherein:

n is 1 to 5;

x, y, and z are each 0 to 11 and y+z≥1; and

x+y+z=2n+1 for a saturated alcohol; or

x+y+z=2n−1 for an unsaturated alcohol.

The alcohol may be selected from the group consisting of fluoromethanol, 2,2,2-trifluoroethanol, 3,3,3-trifluoro-1-propanol, 2,2,3,3-tetrafluoro-1-propanol, 2,2,3,3,4,4,5,5-octafluoropentanol, and 1,1,1,3,3,3-hexafluoro-propan-2-ol.

The catalyst may be an alkaline catalyst and, in particular, may include at least one alkali hydroxide selected from the group consisting of sodium hydroxide and potassium hydroxide and a combination thereof.

The method may further include, after the reacting step, the additional step of separating the product of from the reaction mixture. The reacting step may further include heating the reaction mixture. The reacting step may further include the additional steps of: mixing the alcohol and the catalyst in a reaction vessel; and after the mixing step, adding 1-chloro-3,3,3-trifluoro-propene (1233zd) to the reaction vessel.

The 1-chloro-3,3,3-trifluoro-propene (1233zd) may be either the trans isomer of 1-chloro-3,3,3-trifluoro-propene (1233zd) or the cis isomer of 1-chloro-3,3,3-trifluoro-propene (1233zd).

The product of the method may have the following formula: CF₃—CH₂—CHCl—O—C_(n)H_(x)F_(y)Cl_(z)

wherein:

n is 1 to 5;

x, y, and z are each 0 to 11 and y+z≥1; and

x+y+z=2(n−m)+1, wherein m is an integer of 0 to 2, said method comprising the step of reacting a reaction mixture including an alcohol, a catalyst, and 1-chloro-3,3,3-trifluoro-propene (1233zd).

The alcohol may be an alcohol according to the following formula: C_(n)H_(x)F_(y)Cl_(z)OH

wherein:

n is 1 to 5;

x, y, and z are each 0 to 11 and y+z≥1; and

x+y+z=2n+1 for a saturated alcohol; or

x+y+z=2n−1 for an unsaturated alcohol.

The alcohol may be selected from the group consisting of fluoromethanol, 2,2,2-trifluoroethanol, 3,3,3-trifluoro-1-propanol, 2,2,3,3-tetrafluoro-1-propanol, 2,2,3,3,4,4,5,5-octafluoropentanol, and 1,1,1,3,3,3-hexafluoro-propan-2-ol.

The product of the method may have the following formula: CF₃—CH═CH—O—C_(n)H_(x)F_(y)Cl_(z)

wherein:

n is 1 to 5;

x, y, and z are each 0 to 11 and y+z≥1; and

x+y+z=2(n−m)+1, wherein m is an integer of 0 to 2, said method comprising the step of reacting a reaction mixture including an alcohol, a catalyst, and 1-chloro-3,3,3-trifluoro-propene (1233zd).

The alcohol may be an alcohol according to the following formula: C_(n)H_(x)F_(y)Cl_(z)OH

wherein:

n is 1 to 5;

x, y, and z are each 0 to 11 and y+z≥1; and

x+y+z=2n+1 for a saturated alcohol; or

x+y+z=2n−1 for an unsaturated alcohol.

The alcohol may be selected from the group consisting of fluoromethanol, 2,2,2-trifluoroethanol, 3,3,3-trifluoro-1-propanol, 2,2,3,3-tetrafluoro-1-propanol, 2,2,3,3,4,4,5,5-octafluoropentanol, and 1,1,1,3,3,3-hexafluoro-propan-2-ol.

In another form thereof, the present disclosure provides a liquid composition including at least one solvent selected from formulas (I) and (II): CF₃—CH₂—CHCl—O—C_(n)H_(x)F_(y)Cl_(z)  (I) CF₃—CH═CH—O—C_(n)H_(x)F_(y)Cl_(z)  (II)

and combinations thereof, wherein:

n is 1 to 5;

x, y, and z are each 0 to 11 and y+z≥1; and

x+y+z=2(n−m)+1, wherein m is an integer of 0 to 2, said method comprising the step of reacting a reaction mixture including an alcohol, a catalyst, and 1-chloro-3,3,3-trifluoro-propene (1233zd); and at least one solvent having a boiling point between 20-250° C.

The solvent may have a boiling pint between 20-100° C. or between 25-70° C., and at least one solvent may have an ozone depletion potential (ODP) of not greater than about 0.5.

DETAILED DESCRIPTION

The present disclosure relates to the production of solvents for applications such as heat transfer, cleaning, and degreasing, for example. In particular, the present disclosure relates the production of solvents derived from 1-chloro-3,3,3-trifluoro-propene, such as chloro and/or fluoro substituted alkanes and chloro and/or fluoro substituted trifluoropropenyl ethers.

1-chloro-3,3,3-trifluoro-propene, CF₃CH═CHCl, also known as 1233zd, is a non-flammable, low GWP, low toxicity solvent. The chemical structure of 1233zd is set forth in formula (I) below:

1233zd exists as a trans isomer, as shown in formula (I) above, in which the CF₃ and Cl groups are on opposite sides of the double bond with respect to the longest chain of carbon atoms, and as a cis isomer, shown formula (II) below, in which the CF₃ and Cl groups are on the same side of the double bond with respect to the longest chain of carbon atoms:

The trans isomer has a boiling point of 19° C., while the cis isomer has a boiling point of 40° C.

In order to form useful solvents derived from 1233zd, the 1233zd starting material is reacted with an alcohol and a catalyst according to the overall reaction (1) below, in which the alcohol is exemplified as fluoromethanol (CH₂FOH) and the catalyst is exemplified as potassium hydroxide: CF₃CH═CHCl+CH₂FOH+KOH→CF₃CH═CH—O—CH₂F+KCl+H₂O  (1)

Suitable alcohols for use with the present methods may be generally described by the following chemical formula: C_(n)H_(x)F_(y)Cl_(z)OH

wherein:

n is 1 to 5;

x, y, and z are each 0 to 11, and y+z≥1; and

x+y+z=2n+1 for a saturated alcohol; or

x+y+z=2n−1 for an unsaturated alcohol.

In exemplary embodiments, the alcohol may be a chloro-alcohol, a fluoro-alcohol, or a chloro/fluoro-alcohol, having constituent carbons are at least partially substituted with chlorine, fluorine, or both chlorine and fluorine atoms. Exemplary fluoro-alcohols include, e.g., fluoromethanol (CH₂FOH), 2,2,2-trifluoroethanol (CF₃CH₂OH), 3,3,3-trifluoro-1-propanol (CF₃CH₂CH₂OH), 2,2,3,3-tetrafluoro-1-propanol (CHF₂CF₂CH₂OH), 2,2,3,3,4,4,5,5-octafluoropentanol (CHF₂CF₂CF₂CF₂CH₂OH), and 1,1,1,3,3,3-hexafluoro-propan-2-ol ((CF₃)₂CHOH).

The alcohol functions as a solvent for the reaction, and as a chlorine substituent to replace the chlorine atom of 1233zd to form an alkoxy group.

The catalyst may be an alkaline catalyst, such as an alkali hydroxide including, for example, sodium hydroxide (NaOH) and/or potassium hydroxide (KOH), and functions in part to absorb the chlorine atom which is removed from 1233zd.

In one exemplary embodiment, the molar ratio of 1233zd to alcohol may be 10:1 to 1:20 and the molar ratio of 1233zd to catalyst may be 100:1 to 1:5. In one particular embodiment, the molar ratio of 1233zd to alcohol to catalyst is about 1:4:1.2.

The reaction may be initiated by first combining the catalyst and the alcohol in a reaction vessel, such as an autoclave, with stirring, followed by adding the 1233zd to the reaction vessel with continued stirring.

In a first stage addition reaction, set forth as reaction (2) below and again exemplified in connection with fluoromethanol as the alcohol, the alcohol adds across the double bond of 1233zd, typically with high selectivity for the addition of the alcohol to the number 3 carbon opposite the double bond from the CF₃ group, to form an intermediate alkane: CF₃CH═CHCl+CH₂FOH→CF₃CH₂CHCl—OCH₂F  (2)

Depending on the alcohol used, the carbon(s) of the intermediate alkane may be substituted with chlorine, fluorine, or both chlorine and fluorine. Reaction (2) is exothermic and typically spontaneous, and a cooling medium may be employed during the reaction, such as a cold water bath, for example, or the reaction may be conducted in a cooled environment.

The products of the first stage addition reaction themselves could be final products used as solvents for various applications according to the present disclosure, wherein such products will have molecular weights and boiling points higher than that of 1233zd, the boiling points typically higher than 40° C.

The alkane intermediate products of the first stage addition reaction may be described by the following chemical formula: CF₃—CH₂—CHCl—O—C_(n)H_(x)F_(y)Cl_(z)

wherein:

n is 1 to 5;

x, y, and z are each 0 to 11 and y+z≥1; and

x+y+z=2(n−m)+1, wherein m is an integer of 0 to 2.

In a second stage elimination (or dehydrohalogenation) reaction following reaction (2), set forth as reaction (3) below and again exemplified in connection with fluoromethanol as the alcohol and potassium hydroxide as the catalyst, a trifluoropropene ether is produced when the alkane intermediate loses the chlorine atom and a hydrogen atom to re-form the double bond between the number 2 and 3 carbons: CF₃CH₂CHCl—O—CH₂F+KOH→CF₃CH═CH—OCH₂F+KCl+H₂O  (3)

Thus, in the exemplary reaction (3) above, 3,3,3-trifluloropropenyl fluoromethyl ether is formed which, along with other products disclosed herein, will have molecular weights and boiling points higher than that of 1233zd, the boiling points typically higher than 40° C.

Reaction (3) above is endothermic and, in one embodiment, the reaction vessel may be heated as needed to initiate and/or perpetuate the reaction.

Again, depending on the alcohol used, the number of carbon(s) of the trifluoropropene ether may vary, and may be substituted with chlorine, fluorine, or both chlorine and fluorine.

The trifluoropropene ether products of the second stage elimination reaction may be described by the following chemical formula: CF₃—CH═CH—O—C_(n)H_(x)F_(y)Cl_(z)

wherein:

n is 1 to 5;

x, y, and z are each 0 to 11 and y+z≥1; and

x+y+z=2(n−m)+1, wherein m is an integer of 0 to 2.

The products of the first and second stage reactions may be separated from the reaction mixture and/or other products by suitable means depending on their chemical structure and/or boiling point, such as filtration, extraction with water or other solvent and/or distillation, such as atmospheric distillation and/or reduced pressure distillation, for example.

Several exemplary alcohols, together with their resulting first and second stage reaction products that may be obtained in accordance with the present disclosure, are set forth in the Table I below:

TABLE I Exemplary alcohols and 1^(st) and 2^(nd) stage products 1^(st) stage product 2^(nd) stage product Alcohol (of reaction (2)) (of reaction (3)) Fluoromethanol 1-chloro-3,3,3- 3,3,3-trifluoropropenyl [CH₂FOH] trifluoropropyl fluoromethyl fluoromethyl ether (n = 1, x = 2, y = 1, z = 0) ether or or 1-fluoromethoxy-3,3,3- 1-chloro-1-fluoromethoxy- trifluloropropene 3,3,3-trifluoropropane [CF₃CH═CH—OCH₂F] [CF₃CH₂CHCl—OCH₂F] Difluoromethanol 1-chloro-3,3,3- 3,3,3-trifluoropropenyl [CHF₂OH] trifluoropropyl difluoromethyl ether (n = 1, x = 1, y = 2, z = 0) difluoromethyl ether or or 1-difluoromethoxy-3,3,3- 1-chloro-1- trifluloropropene difluoromethoxy-3,3,3- [CF₃CH═CH—OCHF₂] trifluoropropane [CF₃CH₂CHCl—OCHF₂] 2-fluoroethanol 1-chloro-3,3,3- 3,3,3-trifluoropropenyl 2- [CH₂FCH₂OH] (n = 2, x = 4, trifluoropropyl 2-fluoroethyl fluoroethyl ether y = 1, z = 0) ether or or 1-(2-fluoroethoxy)-3,3,3- 1-chloro-1-(2- trifluloropropene fluoroethoxy)-3,3,3- [CF₃CH═CH—OCH₂CH₂F] trifluoropropane [CF₃CH₂CHCl—OCH₂CH₂F] 2,2-difluoroethanol 1-chloro-3,3,3- 3,3,3-trifluoropropenyl 2,2- [CHF₂CH₂OH] (n = 2, x = 3, trifluoropropyl 2,2- difluoroethyl ether y = 2, z = 0) difluoroethyl ether or or 1-(2,2-difluoroethoxy)-3,3,3- 1-chloro-1-(2,2- trifluloropropene difluoroethoxy)-3,3,3- [CF₃CH═CH—OCH₂CHF₂] trifluoropropane [CF₃CH₂CHCl—OCH₂CHF₂] 2,2,2-trifluoroethanol 1-chloro-3,3,3- 3,3,3-trifluoropropenyl 2,2,2- [CF₃CH₂OH] trifluoropropyl 2,2,2- trifluoroethyl ether (n = 2, x = 2, y = 3, z = 0) trifluoroethyl ether or or 1-(2,2,2-trifluoroethoxy)- 1-chloro-1-(2,2,2- 3,3,3-trifluloropropene trifluoroethoxy)-3,3,3- [CF₃CH═CH—OCH₂CF₃] trifluoropropane [CF₃CH₂CHCl—OCH₂CF₃] 2-fluoroallyl alcohol 1-chloro-3,3,3- 3,3,3-trifluoropropenyl 2- [CH₂═CFCH₂OH] (n = 3, trifluoropropyl 2-fluoroallyl fluoroallyl ether x = 4, y = 1, z = 0) ether or or 1-(2-fluoroallyoxy)-3,3,3- 1-chloro-1-(2- trifluloropropene fluoroallyoxy)-3,3,3- [CF₃CH═CH—OCH₂CH₂CH₂F] trifluoropropane [CF₃CH₂CHCl—OCH₂CH₂CH₂F] 3-fluoro-1-propanol 1-chloro-3,3,3- 3,3,3-trifluoropropenyl 3- [CH₂FCH₂CH₂OH] (n = 3, trifluoropropyl 3- fluoropropyl ether x = 6, y = 1, z = 0) fluoropropyl ether or or 1-(3-fluoropropoxy)-3,3,3- 1-chloro-1-(3- trifluloropropene fluoropropoxy)-3,3,3- [CF₃CH═CH—OCH₂CH₂CH₂F] trifluoropropane [CF₃CH₂CHCl—OCH₂CH₂CH₂F] 2,2-difluoro-1-propanol 1-chloro-3,3,3- 3,3,3-trifluoropropenyl 2,2- [CH₃CF₂CH₂OH] (n = 3, trifluoropropyl 2,2- difluoropropyl ether x = 5, y = 2, z = 0) difluoropropyl ether or or 1-(2,2-difluoropropoxy)- 1-chloro-1-(2,2- 3,3,3-trifluloropropene difluoropropoxy)-3,3,3- [CF₃CH═CH—OCH₂CFS₂CH₃] trifluoropropane [CF₃CH₂CHCl—OCH₂CF₂CH₃] 3,3,3-trifluoro-1-propanol 1-chloro-3,3,3- 3,3,3-trifluoropropenyl 3,3,3- [CF₃CH₂CH₂OH] (n = 3, trifluoropropyl 3,3,3- trifluoropropyl ether x = 4, y = 3, z = 0) trifluoropropyl ether or or 1-(3,3,3-trifluoropropoxy)- 1-chloro-1-(3,3,3- 3,3,3-trifluloropropene trifluoropropoxy)-3,3,3- [CF₃CH═CH—OCH₂CH₂CF₃] trifluoropropane [CF₃CH₂CHCl—OCH₂CH₂CF₃] 2,2,3,3-tetrafluoro-1- 1-chloro-3,3,3- 3,3,3-trifluoropropenyl propanol trifluoropropyl 2,2,3,3- 2,2,3,3-tetrafluoropropyl [CHF₂CF₂CH₂OH] (n = 3, tetrafluoropropyl ether ether x = 3, y = 4, z = 0) or or 1-chloro-1-(2,2,3,3- 1-(2,2,3,3- tetrafluoropropoxy)-3,3,3- tetrafluoropropoxy)-3,3,3- trifluoropropane trifluloropropene [CF₃CH₂CHCl—OCH₂CF₂CHF₂] [CF₃CH═CH—OCH₂CF₂CHF₂] 2,2,3,3,3-pentafluoro-1- 1-chloro-3,3,3- 3,3,3-trifluoropropenyl propanol trifluoropropyl 2,2,3,3,3- 2,2,3,3,3-pentafluoropropyl [CF₃CF₂CH₂OH] (n = 3, pentafluoropropyl ether ether x = 2, y = 5, z = 0) or or 1-chloro-1-(2,2,3,3,3- 1-(2,2,3,3,3- pentafluoropropoxy)-3,3,3- pentafluoropropoxy)-3,3,3- trifluoropropane trifluloropropene [CF₃CH₂CHCl—OCH₂CF₂CF₃] [CF₃CH═CH—OCH₂CF₂CF₃] 1,1,1,3,3,3-hexafluoro-2- 1-chloro-3,3,3- 3,3,3-trifluoropropenyl propanol trifluoropropyl 1,1,1,3,3,3- 1,1,1,3,3,3- [(CF₃)₂CHOH] hexafluoroisopropyl ether hexafluoroisopropyl ether (n = 3, x = 1, y = 6, z = 0) or or 1-chloro-1-(1,1,1,3,3,3- 1-(1,1,1,3,3,3- hexafluoroisopropoxy)- hexafluoroisopropoxy)- 3,3,3-trifluoropropane 3,3,3-trifluloropropene [CF₃CH₂CHCl—OCH(CF₃)₂] [CF₃CH═CH—OCH(CF₃)₂] 2-chloro-1-ethanol 1-chloro-3,3,3- 3,3,3-trifluoropropenyl vinyl [CH₂ClCH₂OH] trifluoropropyl 2- ether (n = 2, x = 4, y = 0, z = 1) chloroethyl ether or or 1-vinyloxy-3,3,3- 1-chloro-1-(2- trifluloropropene chloroethoxy)-3,3,3- [CF₃CH═CH—OCH═CH₂] trifluoropropane [CF₃CH₂CHCl—OCH₂CH₂Cl] 1,3-dichloro-2-propanol 1-chloro-3,3,3- 3,3,3-trifluoropropenyl 1- [(CH₂Cl)₂CHOH] trifluoropropyl 1,3- chloromethylethenyl ether (n = 3, x = 5, y = 0, z = 2) dichloroisopropyl ether or or 1-(1- 1-chloro-1-(1,3- chloromethylethenyloxy)- dichloroisopropoxy)-3,3,3- 3,3,3-trifluloropropene trifluoropropane [CF₃CH═CH—OC(CH₂Cl)═CH₂] [CF₃CH₂CHCl—OCH(CH₂Cl)₂] 2,2,3,4,4,4- 1-chloro-3,3,3- 3,3,3-trifluoropropenyl hexafluorobutanol trifluoropropyl 2,2,3,4,4,4- 2,2,3,4,4,4-hexafluorobutyl [CF₃CHFCF₂CH₂OH] hexafluorobutyl ether (n = 4, x = 3, y = 6, z = 0) ether or or 3,3,3-trifluoropropenyloxy- 1-chloro-1-(3- 2,2,3,4,4,4- fluoropropoxy)- hexafluorobutane 2,2,3,4,4,4- [CF₃CH═CH—OCH₂CF₂CHFCF₃] hexafluorobutane [CF₃CH₂CHCl—OCH₂CF₂CHFCF₃] 2,2,3,3,4,4,4- 1-chloro-3,3,3- 3,3,3-trifluoropropenyl heptafluorobutanol trifluoropropyl 2,2,3,3,4,4,4-hepta [CF₃CF₂CF₂CH₂OH] 2,2,3,3,4,4,4-hepta fluorobutyl (n = 4, x = 2, y = 7, z = 0) fluorobutyl ether ether or or 3,3,3-trifluoropropenyloxy- 1-chloro-1-(3- 2,2,3,3,4,4,4-hepta fluoropropoxy)- fluorobutane 2,2,3,3,4,4,4-hepta [CF₃CH═CH—OCH₂CF₂CHFCF₃] fluorobutane [CF₃CH₂CHCl—OCH₂CF₂CF₂CF₃] 2,2,3,3,4,4,5,5- 1-chloro-3,3,3- 3,3,3-trifluoropropenyl octafluoropentanol trifluoropropyl 2,2,3,3,4,4,5,5- [CHF₂CF₂CF₂CF₂CH₂OH] 2,2,3,3,4,4,5,5- octafluoropentyl (n = 5, x = 2, y = 8, z = 0) octafluoropentyl ether ether or or 3,3,3-trifluoropropenyloxy- 1-chloro-1-(3- 2,2,3,3,4,4,5,5- fluoropropoxy)- octafluoropentane 2,2,3,3,4,4,5,5- [CF₃CH═CH—OCH₂CF₂CF₂CF₂CHF₂] octafluoropentane [CF₃CH₂CHCl—OCH₂CF₂CF₂CF₂CHF₂]

Advantageously, the products of the first and second stage reactions will have a higher molecular weight, and therefore a higher boiling point, than 1233zd and, in many cases, such products will have a boiling point higher than room temperature (between 15° C. and 25° C.), thereby facilitating use of the products as solvents in many potential applications.

The products of the first and second stage reactions, i.e., the disclosed compounds, exhibit one or more, and may exhibit all, of the following properties: chemical stability; no substantial ozone depleting potential (ODP); relatively high degree of miscibility with common contaminants, particularly mineral oil and/or silicone oil; low or no flammability; low or no toxicity; and low or no global warming potential (GWP).

More specifically, the disclosed compounds may have: no substantial ozone depletion potential, preferably an ODP of not greater than about 0.5, not greater than about 0.25, or not greater than about 0.1, a GWP of not greater than about 150, or not greater than about 50.

In many of the embodiments, the disclosed compounds have a normal boiling point as low as 20° C., 25° C., 45° C. or 50° C. or as high as 60° C., 70° C., 100° C. or 250° C., or within any range defined between any two of the foregoing values, such as from 20° C. to 70° C., from 45° C. to 60° C., or from 50° C. to 60° C., for example.

The disclosed compounds may also have no flash point as measured by one of the standard flash point methods, for example ASTM-1310-86 “Flash point of liquids by tag Open-cup apparatus” and an atmospheric lifetime of not greater than about 100 days, such as not greater than about 50 days. Further, the disclosed compound are miscible with greater than 20% by weight of mineral oil and/or silicone oil, such as in a weight ratio in the range of at least about 80:20 to about 20:80, or in substantially all proportions.

The disclosed compounds may exhibit a relatively low toxicity value.

As used herein, ODP is defined in the “Scientific Assessment of Ozone Depletion, 2002”, a report of the World Meteorological association, incorporated herein by reference. As used herein, GWP is defined relative to that of carbon dioxide and over a 100 year time horizon, and defined in the same reference as for the ODP mentioned above. As used herein, miscibility is measured in accordance with visual evaluation of phase formation or separation when two liquids are mixed together, as is known to those skilled in the art.

The disclosed compounds thus generally possess properties and characteristics that are highly desirable for use in connection with many different applications, including many different types of cleaning and contaminant removal applications.

For example, in cleaning applications, the disclosed compounds may be used in liquid compositions, either alone or with one or more co-solvents, as cleaning solvents for greases, oils, waxes and the like, for use in mechanical part cleaning, precision cleaning and/or electronics cleaning, such as cleaning electric motors, compressors, heavy metal parts, delicate precision metal parts, printed circuit boards, gyroscopes, guidance systems, aerospace and missile hardware, aluminum parts and the like. Other applications include degreasing, dry-cleaning, solvent etching, and as a solvent for aerosols or other sprayable compositions, as carrier solvents for lubricants, or other surface treatment applications.

For example, in degreasing operations, the disclosed compounds may be used as solvents in vapor degreasing methods, in which an article to be cleaned is exposed to a solvent vapor, preferably at or above room temperature, to remove grease or other contaminants from the surface of the article or alternatively, in liquid degreasing operations, in which an article to be cleaned is exposed to the solvent in liquid form by immersing the article in the liquid solvent, typically at an elevated temperature approaching the boiling point of the solvent.

In one particular application, the solvents disclosed herein may be formulated with other components, such as a C₁-C₃ alcohol and/or a C₄-C₆ hydrocarbon, to form a composition useful for removing ink or ink-based markings from the surfaces of articles of manufacture, such as optical lenses, electro-mechanical or electrical parts, before the parts are packaged and commercially sold without damaging the underlying surfaces of the articles themselves. The articles and their surfaces may be metal or metal-based, cellulose-based, silica-based, or made from a plastic polymeric material, and the solvents may be in the form of a liquid, aerosol and/or sprayable composition.

The disclosed compounds may also be used as a heat transfer medium, flame suppressing agent, or foam blowing agent, for example. In particular, the disclosed compounds may be used as heat transfer fluids in methods and systems for transferring heat, such as refrigerants used in refrigeration, air conditioning and heat pump systems, and well as fire suppressants, such as additives to reduce the flammability of fluids, and as components involved in the formation of foam, foam premixes, foam products and blowing agents for foams.

Further details regarding exemplary applications of the disclosed compounds are disclosed in U.S. Pat. No. 7,985,299, assigned to the assignee of the present invention, the entire disclosure of which is incorporated by reference herein.

While this invention has been described as having exemplary designs, the present invention can be further modified within the spirit and scope of this disclosure. This application is therefore intended to cover any variations, uses, or adaptations of the invention using its general principles. Further, this application is intended to cover such departures from the present disclosure as come within known or customary practice in the art to which this invention pertains and which fall within the limits of the appended claims. 

The invention claimed is:
 1. A liquid composition comprising at least one solvent selected from formulas (I) and (II): CF₃—CH₂—CHCl—O—C_(n)H_(x)F_(y)Cl_(z)  (I) CF₃—CH═CH—O—C_(n)H_(x)F_(y)Cl_(z)  (II) and combinations thereof, wherein: n is 1 to 5; x, y, and z are each 0 to 11 and y+z≥1; and x+y+z=2(n−m)+1, wherein m is an integer of 0 to 2, wherein the at least one solvent selected from formulas (I) and (II) is made by the method comprising the step of reacting a reaction mixture including an alcohol, a catalyst, and 1-chloro-3,3,3-trifluoro-propene (1233zd); and the at least one solvent having a boiling point from 20° C. to 250° C.
 2. The liquid composition of claim 1, wherein the at least one solvent has a boiling point from 20° C. to 100° C.
 3. The liquid composition of claim 1, wherein the at least one solvent has a boiling point from 25° C. to 70° C.
 4. The liquid composition of claim 1, wherein the at least one solvent has an ozone depletion potential (ODP) of not greater than about 0.5.
 5. The liquid composition of claim 1, further comprising at least one additional solvent in the form of a C₁-C₃ alcohol.
 6. The liquid composition of claim 1, further comprising at least one additional solvent in the form of a C₄-C₆ hydrocarbon.
 7. The liquid composition of claim 1, wherein the at least one solvent has the following formula: CF₃—CH₂—CHCl—O—C_(n)H_(x)F_(y)Cl_(z) wherein: n is 1 to 5; x, y, and z are each 0 to 11 and y+z≥1; and x+y+z=2(n−m)+1, wherein m is an integer of 0 to
 2. 8. The liquid composition of claim 7, wherein the at least one solvent has a boiling point from 20° C. to 100° C.
 9. The liquid composition of claim 7, wherein the at least one solvent has a boiling point from 25° C. to 70° C.
 10. The liquid composition of claim 7, wherein the at least one solvent has an ozone depletion potential (ODP) of not greater than about 0.5.
 11. The liquid composition of claim 7, further comprising at least one additional solvent in the form of a C₁-C₃ alcohol.
 12. The liquid composition of claim 7, further comprising at least one additional solvent in the form of a C₄-C₆ hydrocarbon.
 13. The liquid composition of claim 1, wherein the at least one solvent has the following formula: CF₃—CH═CH—O—C_(n)H_(x)F_(y)Cl_(z) wherein: n is 1 to 5; x, y, and z are each 0 to 11 and y+z≥1; and x+y+z=2(n−m)+1, wherein m is an integer of 0 to
 2. 14. The liquid composition of claim 13, wherein the at least one solvent has a boiling point from 20° C. to 100° C.
 15. The liquid composition of claim 13, wherein the at least one solvent has a boiling point from 25° C. to 70° C.
 16. The liquid composition of claim 13, wherein the at least one solvent has an ozone depletion potential (ODP) of not greater than about 0.5.
 17. The liquid composition of claim 13, further comprising at least one additional solvent in the form of a C₁-C₃ alcohol.
 18. The liquid composition of claim 13, further comprising at least one additional solvent in the form of a C₄-C₆ hydrocarbon. 